Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm 		0.600 CausalMutation CGI

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.540 Biomarker CTD_human

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm 		0.510 Biomarker CTD_human

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm 		0.510 CausalMutation CGI

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0022603
Disease: Seborrheic keratosis
Seborrheic keratosis 		0.500 CausalMutation CLINVAR

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		0.500 CausalMutation CGI

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.500 CausalMutation CGI

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.500 GeneticVariation UNIPROT

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor 		0.500 Biomarker CTD_human

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.460 CausalMutation CLINVAR

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.460 CausalMutation CGI

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0265529
Disease: Plagiocephaly
Plagiocephaly 		0.420 Biomarker HPO

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0175699
Disease: Saethre-Chotzen Syndrome
Saethre-Chotzen Syndrome 		0.410 CausalMutation CLINVAR

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0175699
Disease: Saethre-Chotzen Syndrome
Saethre-Chotzen Syndrome 		0.410 GeneticVariation ORPHANET

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		0.410 Biomarker HPO

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.410 Biomarker HPO

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.410 Biomarker GENOMICS_ENGLAND

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.410 GeneticVariation CLINVAR

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		0.400 Biomarker HPO

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		0.400 Biomarker HPO

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0685381
Disease: Congenital hypoplasia of radius
Congenital hypoplasia of radius 		0.400 Biomarker GENOMICS_ENGLAND

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0685381
Disease: Congenital hypoplasia of radius
Congenital hypoplasia of radius 		0.400 Biomarker HPO

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.340 CausalMutation CGI

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.300 Biomarker CTD_human

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		0.300 Biomarker MGD